Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCTGCTCCAACCCCAACCACCGCA[A/C]CCCTACGCTGACCAGGTGAGTAGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 102578 MIM: 608326 | ||||||||||||||||||||
Literature Links: |
PML PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
PML - promyelocytic leukemia | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002675.3 | 727 | Missense Mutation | AAC,ACC | N,T 196 | NP_002666.1 | |
NM_033238.2 | 727 | Missense Mutation | AAC,ACC | N,T 196 | NP_150241.2 | |
NM_033239.2 | 727 | Missense Mutation | AAC,ACC | N,T 196 | NP_150242.1 | |
NM_033240.2 | 727 | Missense Mutation | AAC,ACC | N,T 196 | NP_150243.2 | |
NM_033244.3 | 727 | Missense Mutation | AAC,ACC | N,T 196 | NP_150247.2 | |
NM_033246.2 | 727 | Missense Mutation | AAC,ACC | N,T 196 | NP_150249.1 | |
NM_033247.2 | 727 | Missense Mutation | AAC,ACC | N,T 196 | NP_150250.2 | |
NM_033249.2 | 727 | Missense Mutation | AAC,ACC | N,T 196 | NP_150252.1 | |
NM_033250.2 | 727 | Missense Mutation | AAC,ACC | N,T 196 | NP_150253.2 |
STOML1 - stomatin like 1 | ||||||
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There are no transcripts associated with this gene. |